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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535046생성일: 2026년 10월 25일

Water → 1-benzyl 4-methyl (2S)-2-[benzyl((2S)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinate

https://huagongshe.com/reaction/535046

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium FluorideHCID 5235—
반응물Oxiranemethanol, 4-methylbenzenesulfonate, (S)-HCID 153296—
반응물TrimethylaluminumHCID 16682925—
반응물Acetone cardiceHCID 18522661—
반응물(S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl esterHCID 67303755—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물1-benzyl 4-methyl (2S)-2-[benzyl((2S)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinateHCID 8734866891.8%

반응 조건

온도-78 °C

반응 단계

To a solution of (2S)-(+)-glycidyl tosylate (23.0 g, 0.101 mol) in 500 mL of methylene chloride was added 2.00 M of trimethylaluminum in toluene (50.4 mL) at −78 Celsius, under an atmosphere of nitrogen. After stirred at −78 Celsius for 10 min, to the mixture was added a solution of (S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl ester (30.0 g, 0.0916 mol) in 150 mL of methylene chloride. The resulting reaction mixture was stirred at −78 Celsius for 30 min. The dry ice-acetone bath was changed to an ice-water bath to warm the mixture up to 0 Celsius. The mixture was stirred at 0 Celsius for 30 min. To the reaction mixture was added sodium fluoride (16.2 g, 0.385 mol) followed by water (10.4 mL, 0.577 mol) at 0 Celsius. The resulting suspension was rapidly stirred for 1 h at 0 Celsius and filtered through a short column of celite and the column was subsequently washed with 600 mL of methylene chloride. The combined filtrates were dried over sodium sulfate, concentrated to dry and purified by column purification (eluting with 0 to 20% EtOAc in hexane) to yield the titled compound (46.7 g, 91.7%). MS (ESI): (M+H)+=556.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853243B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-2f6ffbcd435a4f7da3859880e24c9c1e
출처 메모uspto-grants-2014_10